Human (GRCh38.p14)
Description

minichromosome maintenance complex component 2 [Source:HGNC Symbol;Acc:HGNC:6944]

Gene Synonyms

BM28, CCNL1, CDC19, CDCL1, D3S3194, DFNA70, KIAA0030

Location

Chromosome 3: 127,598,410-127,622,436 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 9 transcripts (splice variants), 205 orthologues, 8 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000265056.12MCM2-2013434904aaENSP00000265056.7
 
Protein coding
CCDS3043P49736 NM_004526.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000491422.1MCM2-2092844836aaENSP00000420528.1
 
Protein coding
H0Y8E6 -TSL:5CDS 5' incomplete
ENST00000480910.1MCM2-208693128aaENSP00000419802.1
 
Protein coding
C9JZ21 -TSL:2CDS 3' incomplete
ENST00000472731.1MCM2-204547103aaENSP00000418930.1
 
Protein coding
C9J013 -TSL:2CDS 3' incomplete
ENST00000474964.5MCM2-2062847146aaENSP00000420007.1
 
Nonsense mediated decay
F8WDM3 -TSL:2
ENST00000477668.5MCM2-207251091aaENSP00000417800.1
 
Nonsense mediated decay
H7C4N9 -TSL:2CDS 5' incomplete
ENST00000468414.1MCM2-2021076No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000468659.1MCM2-203557No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000473785.1MCM2-205684No protein-
 
Retained intron
--TSL:2